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藻蓝蛋白支架对生长因子相关细胞迁移在皮肤创伤愈合中的调控作用。

Regulation of growth factors-associated cell migration by C-phycocyanin scaffold in dermal wound healing.

机构信息

Department of Applied Physiology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

出版信息

Clin Exp Pharmacol Physiol. 2012 Jan;39(1):13-9. doi: 10.1111/j.1440-1681.2011.05627.x.

Abstract
  1. The present study examined the role of C-phycocyanin (C-pc) in relation to growth factors and cell migration during wound healing. 2. Histological and biochemical studies showed that C-pc scaffold significantly (P < 0.01) increased hydroxyl proline, total hexamine and protein content, and decreased uronic acid content in the wound tissues during a time course study in newly formed skin. 3. Reverse transcription polymerase chain reaction array of mouse growth factors in wound tissue showed overexpression (up to 10-fold) of growth factors, such as Cxcl12, Fgf18, Lefty 1, Lefty 2, Rabep 1 and Zip91, and downregulation (up to -10-fold) of Amh, Bmp 7 and Nodal genes in a 6-day period in C-pc treated groups. Also, Csf 3, Fgf 22, Mdk, Igf 2, transforming growth factor (TGF)-α 1 and interleukin (IL)-1β showed an upregulation of more than 30-fold than the control groups. TGF-β subfamily cytokine growth factors, such as Bmp 2, 4 and 8b, and other growth factors, such as Cxcl 1, showed the highest activity on day 3, showing a transient type of regulation. Western blot analysis showed a positive correlation between gene activity and protein expressions of Bmp 8b, Bmp4, Bmp2 and Cxcl 1. Day 6 in the C-pc group showed the highest csf3 and IL-1β expression. 4. C-pc had no direct effect on keratinocyte migration. However, keratinocytes that were co-cultured with fibroblasts showed a significantly higher rate of migration in the presence of C-pc, showing an indirect effect of C-pc on keratinocyte migration. 5. In conclusion, biodegradable C-pc scaffold might help to serve as an alternate scaffold material for wound healing.
摘要
  1. 本研究探讨了 C-藻蓝蛋白(C-pc)在生长因子和细胞迁移与伤口愈合中的作用。

  2. 组织学和生物化学研究表明,在新形成的皮肤中,C-pc 支架在时间过程研究中显著(P < 0.01)增加了羟基脯氨酸、总己糖胺和蛋白质含量,降低了伤口组织中的糖醛酸含量。

  3. 伤口组织中鼠生长因子的逆转录聚合酶链反应阵列显示,在 C-pc 处理组中,生长因子如 Cxcl12、Fgf18、Lefty 1、Lefty 2、Rabep 1 和 Zip91 的表达过度(高达 10 倍),而 Amh、Bmp 7 和 Nodal 基因的表达下调(高达-10 倍)在 6 天内。此外,Csf3、Fgf22、Mdk、Igf2、转化生长因子(TGF)-α1 和白细胞介素(IL)-1β的表达水平比对照组高出 30 多倍。TGF-β亚家族细胞因子生长因子,如 Bmp 2、4 和 8b,以及其他生长因子,如 Cxcl 1,在第 3 天表现出最高的活性,表现出一种短暂的调节类型。Western blot 分析显示,Bmp 8b、Bmp4、Bmp2 和 Cxcl 1 的基因活性与蛋白表达之间存在正相关。在 C-pc 组第 6 天,csf3 和 IL-1β的表达最高。

  4. C-pc 对角质形成细胞迁移没有直接影响。然而,与成纤维细胞共培养的角质形成细胞在 C-pc 存在的情况下表现出更高的迁移率,这表明 C-pc 对角质形成细胞迁移有间接影响。

  5. 总之,可生物降解的 C-pc 支架可能有助于作为伤口愈合的替代支架材料。

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